Canonical Allele Identifier: CA376146713

Gene: CUBN

Linked Data

• gnomAD v4: 10-16915961-T-C
• MyVariant Identifiers: chr10:g.16957960T>C (hg19) ; chr10:g.16915961T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915961T>C , CM000672.2:g.16915961T>C	GRCh38
NC_000010.10:g.16957960T>C , CM000672.1:g.16957960T>C	GRCh37
NC_000010.9:g.16997966T>C	NCBI36
NG_008967.1:g.218857A>G , LRG_540:g.218857A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7070A>G MANE Select	ENSP00000367064.4:p.Tyr2357Cys
ENST00000377833.8:c.7070A>G	ENSP00000367064.4:p.Tyr2357Cys
NM_001081.3:c.7070A>G , LRG_540t1:c.7070A>G	NP_001072.2:p.Tyr2357Cys
XM_011519708.1:c.7070A>G	XP_011518010.1:p.Tyr2357Cys
XM_011519709.1:c.3056A>G	XP_011518011.1:p.Tyr1019Cys
XM_011519710.1:c.3032A>G	XP_011518012.1:p.Tyr1011Cys
XM_011519711.1:c.2912A>G	XP_011518013.1:p.Tyr971Cys
XM_011519708.2:c.7070A>G	XP_011518010.1:p.Tyr2357Cys
XM_011519709.2:c.3056A>G	XP_011518011.1:p.Tyr1019Cys
XM_011519710.2:c.3032A>G	XP_011518012.1:p.Tyr1011Cys
XM_011519711.3:c.2912A>G	XP_011518013.1:p.Tyr971Cys
NM_001081.4:c.7070A>G MANE Select	NP_001072.2:p.Tyr2357Cys